Diversity and composition of the microbiome associated with eggs of the Southern green stinkbug, Nezara viridula (Hemiptera: Pentatomidae)

IF 3.9 3区 生物学 Q2 MICROBIOLOGY MicrobiologyOpen Pub Date : 2022-12-07 DOI:10.1002/mbo3.1337
Margot W. J. Geerinck, Sara Van Hee, Gabriele Gloder, Sam Crauwels, Stefano Colazza, Hans Jacquemyn, Antonino Cusumano, Bart Lievens
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引用次数: 4

Abstract

Although microbial communities of insects from larval to adult stage have been increasingly investigated in recent years, little is still known about the diversity and composition of egg-associated microbiomes. In this study, we used high-throughput amplicon sequencing and quantitative PCR to get a better understanding of the microbiome of insect eggs and how they are established using the Southern green stinkbug Nezara viridula (L.) (Hemiptera: Pentatomidae) as a study object. First, to determine the bacterial community composition, egg masses from two natural populations in Belgium and Italy were examined. Subsequently, microbial community establishment was assessed by studying stinkbug eggs of different ages obtained from laboratory strains (unlaid eggs collected from the ovaries, eggs less than 24 h old, and eggs collected 4 days after oviposition). Both the external and internal egg-associated microbiomes were analyzed by investigating egg washes and surface-sterilized washed eggs, respectively. Eggs from the ovaries were completely devoid of bacteria, indicating that egg-associated bacteria were deposited on the eggs during or after oviposition. The bacterial diversity of deposited eggs was very low, with on average 6.1 zero-radius operational taxonomic units (zOTUs) in the external microbiome and 1.2 zOTUs in internal samples of egg masses collected from the field. Bacterial community composition and density did not change significantly over time, suggesting limited bacterial growth. A Pantoea-like symbiont previously found in the midgut of N. viridula was found in every sample and generally occurred at high relative and absolute densities, especially in the internal egg samples. Additionally, some eggs harbored a Sodalis symbiont, which has previously been found in the abdomen of several insects, but so far not in N. viridula populations. We conclude that the egg-associated bacterial microbiome of N. viridula is species-poor and dominated by a few symbionts, particularly the species-specific obligate Pantoea-like symbiont.

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南方绿臭虫(Nezara viridula)虫卵微生物群的多样性和组成(半翅目:蝽科)
近年来,人们对昆虫从幼虫到成虫阶段的微生物群落进行了越来越多的研究,但对与卵相关的微生物群落的多样性和组成知之甚少。本研究以南方绿臭虫Nezara viridula (L.)(半翅目:Pentatomidae)为研究对象,采用高通量扩增子测序和定量PCR技术,深入了解虫卵微生物组及其建立机制。首先,为了确定细菌群落组成,研究人员检查了比利时和意大利两个自然种群的鸡蛋质量。随后,通过研究实验室菌株不同年龄的臭虫卵(从卵巢采集的未产卵卵、小于24 h的卵和产卵后4 d采集的卵)来评估微生物群落的建立。通过对洗蛋液和表面消毒的洗蛋液,分别分析了外部和内部鸡蛋相关微生物组。来自卵巢的卵完全没有细菌,表明与卵相关的细菌在产卵期间或产卵后沉积在卵上。产卵卵的细菌多样性很低,野外采集的卵团体外微生物群平均为6.1个零半径操作分类单位(zero-radius operational taxonomic units, zOTUs),体内微生物群平均为1.2个。细菌群落组成和密度随时间变化不明显,表明细菌生长有限。在每个样本中都发现了一种在病毒乳杆菌中肠中发现的泛菌状共生体,并且通常以较高的相对密度和绝对密度出现,特别是在内部卵样本中。此外,一些卵还含有一种共生体,这种共生体以前在几种昆虫的腹部被发现,但到目前为止还没有在N. viridula种群中发现。我们得出结论,病毒乳杆菌的卵相关细菌微生物组是物种贫乏的,由少数共生体主导,特别是种特异性的专性pantoea样共生体。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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